BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    3M CUROS CAP

    MDR report key: 23544340 · Received November 12, 2025

    Report

    Report Number
    MW5178826
    Event Type
    Malfunction
    Date Received
    November 12, 2025
    Date of Event
    November 4, 2025
    Report Date
    November 7, 2025
    Manufacturer
    3M COMPANY
    Product Code
    QBP
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    FEMALE CUROS CAP BROKE APART WHEN PLACED ON IV LINE. INNER CIRCLE STAYED ON IV END AND THE CAP PART FELL OFF.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2140105 3M CUROS CAP CAP, DEVICE DISINFECTANT QBP 3M COMPANY CFF10-250 12514849

    Patients

    Seq Age Sex Outcome Treatment
    1 60 YR Female Other